Epoxide based inhibitors of the hepatitis C virus non-structural 2 autoprotease

od Shaw, Joseph, Fishwick, Colin W.G., Harris, Mark
Izdano u Antiviral Res (2015)

Identification of a lead like inhibitor of the hepatitis C virus non-structural NS2 autoprotease

od Shaw, Joseph, Harris, Mark, Fishwick, Colin W.G.
Izdano u Antiviral Res (2015)

Linezolid and Tiamulin Cross-Resistance in Staphylococcus aureus Mediated by Point Mutations in the Peptidyl Transferase Center

od Miller, Keith, Dunsmore, Colin J., Fishwick, Colin W. G., Chopra, Ian
Izdano 2008

Identification of an Indazole-Based Pharmacophore for the Inhibition of FGFR Kinases Using Fragment-Led de Novo Design

od Turner, Lewis D., Summers, Abbey J., Johnson, Laura O., Knowles, Margaret A., Fishwick, Colin W. G.
Izdano u ACS Med Chem Lett (2017)

Selective Phosphonylation of 5′-Adenosine Monophosphate (5′-AMP) via Pyrophosphite [PPi(III)]

od Kaye, Karl, Bryant, David E., Marriott, Katie E. R., Ohara, Shohei, Fishwick, Colin W. G., Kee, Terence P.
Izdano u Orig Life Evol Biosph (2016)

Activity of and Development of Resistance to Corallopyronin A, an Inhibitor of RNA Polymerase

od Mariner, Katherine, McPhillie, Martin, Trowbridge, Rachel, Smith, Catriona, O'Neill, Alex J., Fishwick, Colin W. G., Chopra, Ian
Izdano 2011

Determinants of Hepatitis C Virus p7 Ion Channel Function and Drug Sensitivity Identified In Vitro

od StGelais, Corine, Foster, Toshana L., Verow, Mark, Atkins, Elizabeth, Fishwick, Colin W. G., Rowlands, David, Harris, Mark, Griffin, Stephen
Izdano 2009

Furanyl-Rhodanines Are Unattractive Drug Candidates for Development as Inhibitors of Bacterial RNA Polymerase

od Mariner, Katherine R., Trowbridge, Rachel, Agarwal, Anil K., Miller, Keith, O'Neill, Alex J., Fishwick, Colin W. G., Chopra, Ian
Izdano 2010

Structure-Based Identification and Characterization of Inhibitors of the Epilepsy-Associated K(Na)1.1 (KCNT1) Potassium Channel

od Cole, Bethan A., Johnson, Rachel M., Dejakaisaya, Hattapark, Pilati, Nadia, Fishwick, Colin W.G., Muench, Stephen P., Lippiat, Jonathan D.
Izdano u iScience (2020)

Structure-switching M(3)L(2) Ir(iii) coordination cages with photo-isomerising azo-aromatic linkers

od Oldknow, Samuel, Martir, Diego Rota, Pritchard, Victoria E., Blitz, Mark A., Fishwick, Colin W. G., Zysman-Colman, Eli, Hardie, Michaele J.
Izdano u Chem Sci (2018)

Structure-Based Ligand Design of Novel Bacterial RNA Polymerase Inhibitors

od McPhillie, Martin J., Trowbridge, Rachel, Mariner, Katherine R., O’Neill, Alex J., Johnson, A. Peter, Chopra, Ian, Fishwick, Colin W. G.
Izdano 2011

The First Small-Molecule Inhibitors of Members of the Ribonuclease E Family

od Kime, Louise, Vincent, Helen A., Gendoo, Deena M. A., Jourdan, Stefanie S., Fishwick, Colin W. G., Callaghan, Anastasia J., McDowall, Kenneth J.
Izdano u Sci Rep (2015)

Erratum: The First Small-Molecule Inhibitors of Members of the Ribonuclease E Family

od Kime, Louise, Vincent, Helen A., Gendoo, Deena M. A., Jourdan, Stefanie S., Fishwick, Colin W. G., Callaghan, Anastasia J., McDowall, Kenneth J.
Izdano u Sci Rep (2015)

In Silico Design and Biological Evaluation of a Dual Specificity Kinase Inhibitor Targeting Cell Cycle Progression and Angiogenesis

od Latham, Antony M., Kankanala, Jayakanth, Fearnley, Gareth W., Gage, Matthew C., Kearney, Mark T., Homer-Vanniasinkam, Shervanthi, Wheatcroft, Stephen B., Fishwick, Colin W. G., Ponnambalam, Sreenivasan
Izdano u PLoS One (2014)

Identification of Selective Inhibitors of the Potassium Channel Kv1.1–1.2((3)) by High-Throughput Virtual Screening and Automated Patch Clamp

od Wacker, Sören J, Jurkowski, Wiktor, Simmons, Katie J, Fishwick, Colin W G, Johnson, A Peter, Madge, David, Lindahl, Erik, Rolland, Jean-Francois, de Groot, Bert L
Izdano 2012

Assay Platform for Clinically Relevant Metallo-β-lactamases

od van Berkel, Sander S., Brem, Jürgen, Rydzik, Anna M., Salimraj, Ramya, Cain, Ricky, Verma, Anil, Owens, Raymond J., Fishwick, Colin W. G., Spencer, James, Schofield, Christopher J.
Izdano 2013

X-ray and cryo-EM structures of inhibitor-bound cytochrome bc (1) complexes for structure-based drug discovery

od Amporndanai, Kangsa, Johnson, Rachel M., O’Neill, Paul M., Fishwick, Colin W. G., Jamson, Alexander H., Rawson, Shaun, Muench, Stephen P., Hasnain, S. Samar, Antonyuk, Svetlana V.
Izdano u IUCrJ (2018)

Structure Guided Development of Potent Reversibly Binding Penicillin Binding Protein Inhibitors

od Woon, Esther C. Y., Zervosen, Astrid, Sauvage, Eric, Simmons, Katie J., Živec, Matej, Inglis, Steven R., Fishwick, Colin W. G., Gobec, Stanislav, Charlier, Paulette, Luxen, André, Schofield, Christopher J.
Izdano 2011

Structural basis of metallo-β-lactamase, serine-β-lactamase and penicillin-binding protein inhibition by cyclic boronates

od Brem, Jürgen, Cain, Ricky, Cahill, Samuel, McDonough, Michael A., Clifton, Ian J., Jiménez-Castellanos, Juan-Carlos, Avison, Matthew B., Spencer, James, Fishwick, Colin W. G., Schofield, Christopher J.
Izdano u Nat Commun (2016)

Cyclic Boronates Inhibit All Classes of β-Lactamases

od Cahill, Samuel T., Cain, Ricky, Wang, David Y., Lohans, Christopher T., Wareham, David W., Oswin, Henry P., Mohammed, Jabril, Spencer, James, Fishwick, Colin W. G., McDonough, Michael A., Schofield, Christopher J., Brem, Jürgen
Izdano u Antimicrob Agents Chemother (2017)